Test Price
2,800 AED✅ Home Collection Available
ACP2 Gene Lysosomal Acid Phosphatase Deficiency Genetic Test - 2,800 AED
Executive Summary & Core Metrics
- ✓ Diagnostic Accuracy: 99.9% sensitivity via ISO‑accredited NGS processing with orthogonal confirmation of pathogenic variants.
- ✓ Premium Logistics: VIP Mobile Phlebotomy & Temperature‑Controlled Cold‑Chain Home Collection (Available daily from 8 AM to 11 PM).
- ✓ Post‑Test Clinical Guidance: Telephonic interpretation by DHA‑licensed genetics specialist included.
- ✓ Insurance & Billing: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
This next‑generation sequencing test screens the entire coding region of the ACP2 gene, identifying point mutations, small indels, and copy‑number variations linked to lysosomal acid phosphatase deficiency – a metabolic storage disorder. With a 3‑4‑week turnaround and clinical reporting aligned to DHA standards, it is the definitive molecular confirmation for at‑risk families.
| Feature | Our ACP2 NGS Test | Closest Alternative |
|---|---|---|
| Precision / Accuracy | 99.9% diagnostic sensitivity; full gene coverage with 100x depth | ~82% sensitivity for enzyme‑assay based screening |
| Methodology | NGS (Next‑Generation Sequencing) & ACMG variant interpretation | Lysosomal enzyme activity assay (biochemical) |
| Turnaround Time | 3–4 weeks from sample receipt | 4–6 weeks (often requires multiple sample types) |
| Clinical Reporting | DHA‑compliant molecular report with therapy‑guided annotations | Basic enzyme level with no mutation identification |
Physician Insight & Safety Protocols
"Every genetic result carries a human story. As a consultant in medical genetics, I understand the uncertainty families face. This test provides a clear molecular answer, yet no single result replaces thorough clinical evaluation. Please involve your managing physician before any medical decision."
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403Advisory: Essential Precautions Before Testing
Important Safety Notice: This genetic test requires a blood draw of 4 mL via routine venipuncture. Ensure you are well-hydrated and have no active infections. Discontinue any anticoagulants only under physician guidance. Pre-test genetic counseling is mandatory to discuss implications and obtain informed consent in accordance with Federal Decree-Law No. 4 of 2016 on Medical Liability.
Exclusion Criteria & Emergency Red Flags
- Exclusion Criteria: Pregnancy, recent blood transfusion (< 90 days), hematopoietic stem cell transplant within 6 months, active febrile illness.
- Red Flags (seek immediate care): Acute metabolic decompensation, severe acidosis, altered consciousness, tachypnoea, or signs of multi‑organ involvement.
Patient FAQ & Clinical Guidance
1. What exactly does the ACP2 gene test detect?
The ACP2 NGS test identifies DNA mutations in the lysosomal acid phosphatase gene that cause metabolic storage deficiency. It simultaneously screens for single nucleotide variants, small insertions/deletions, and copy number alterations across all coding exons. The report shows pathogenic, likely pathogenic, and variants of uncertain significance following ACMG guidelines.
2. How is the sample collected and when will I receive results?
A certified phlebotomist draws 4 mL of whole blood at your home; results are delivered in 3–4 weeks. The sample is transported under cold‑chain ISO protocols within 4 hours. Pre‑test genetic counselling is mandatory to prepare a family pedigree chart. You will be assigned a clinical coordinator who updates you weekly.
3. Is this test suitable for children and what do positive results mean?
Yes, the test can be performed on minors with parental consent in accordance with UAE medical liability laws. A positive result confirms the diagnosis of lysosomal acid phosphatase deficiency. In children, timely genetic confirmation enables early metabolic intervention and family planning. Positive results are explained during a tele‑consultation, and actionable management pathways are outlined. Genetic data is stored under UAE PDPL protections.
UAE Regulatory & Data Privacy Adherence
DHA‑Compliant & Data Protected
This service strictly adheres to Federal Decree‑Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. All genetic data remains in UAE servers. Facility licensed under DHA License Number: 1143. Clinical supervision: Lina Osama Zaki Quteineh, Consultant Medical Genetics (DHA 9294403). 24‑hour WhatsApp support: +971 54 548 8731.
Clinical & Logistical Metadata
| Test Name | ACP2 Gene Lysosomal Acid Phosphatase Deficiency Genetic Test |
| Price (AED) | 2,800 |
| Turnaround Time | 3–4 weeks from sample receipt |
| Sample Type / Matrix | Whole blood (4 mL in EDTA tube) |
| Methodology Used | Next‑Generation Sequencing (NGS) with full gene coverage and ACMG classification |
| ICD-10-CM Code | E77.8 |
| LOINC Code | 92851-1 |
| DHA Facility License | License No. 1143, Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians